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1.
Journal of Korean Medical Science ; : 605-612, 2017.
Article in English | WPRIM | ID: wpr-49319

ABSTRACT

The purpose of this study was to assess the incidence of spontaneous renal artery dissection (SRAD) as a cause of acute renal infarction, and to evaluate the clinical and multidetector computed tomography (MDCT) findings of SRAD. From November 2011 to January 2014, 35 patients who were diagnosed with acute renal infarction by MDCT were included. We analyzed the 35 MDCT data sets and medical records retrospectively, and compared clinical and imaging features of SRAD with an embolism, using Fisher's exact test and the Mann-Whitney test. The most common cause of acute renal infarction was an embolism, and SRAD was the second most common cause. SRAD patients had new-onset hypertension more frequently than embolic patients. Embolic patients were found to have increased C-reactive protein (CRP) more often than SRAD patients. Laboratory results, including tests for lactate dehydrogenase (LDH) and blood urea nitrogen (BUN), and the BUN/creatinine ratio (BCR) were significantly higher in embolic patients than SRAD patients. Bilateral renal involvement was detected in embolic patients more often than in SRAD patients. MDCT images of SRAD patients showed the stenosis of the true lumen, due to compression by a thrombosed false lumen. None of SRAD patients progressed to an estimated glomerular filtration rate < 60 mL/min/1.73 m2 or to end-stage renal disease during the follow-up period. SRAD is not a rare cause of acute renal infarction, and it has a benign clinical course. It should be considered in a differential diagnosis of acute renal infarction, particularly in patients with new-onset hypertension, unilateral renal involvement, and normal ranges of CRP, LDH, BUN, and BCR.

2.
General Medicine ; : 126-129, 2013.
Article in English | WPRIM | ID: wpr-375237

ABSTRACT

Spontaneous renal artery dissection (SRAD) is uncommon and hence diagnosis is often delayed when ideally a quick one is preferred. We report a case of a 53 year-old male, with a known history of nephrolithiasis, who was admitted into hospital complaining of sudden onset left-sided back pain. Ultrasound showed a right-sided calculus instead of the expected left. A subsequent contrast computed tomography (CT) scan was done showing an infarcted segment of the left kidney. Further investigation with angiography and intravascular ultrasound (IVUS) revealed the presence of two left renal arteries with the distal originating left renal artery having dissected.

3.
Korean Journal of Urology ; : 376-378, 2008.
Article in English | WPRIM | ID: wpr-159176

ABSTRACT

A previously healthy 44-year-old woman, with no notable medical history developed left flank pain. To rule out left renal infarction, enhanced abdominal computed tomography(CT) was done and a wedge shaped hypointense lesion was identified in the left posteromedial aspect of the interpolar region. Renal angiography revealed an isolated renal artery dissection that was causing renal infarction due to narrowing of the main stem of the left renal artery. The patient experienced pain with severe uncontrolled hypertension. The patient was successfully treated by percutaneous angioplasty and renal artery stenting.


Subject(s)
Adult , Female , Humans , Angiography , Angioplasty , Flank Pain , Hypertension , Infarction , Renal Artery
4.
Korean Journal of Nephrology ; : 815-819, 2004.
Article in Korean | WPRIM | ID: wpr-154473

ABSTRACT

Isolated spontaneous renal artery dissection (SRAD) associated with fibromuscular dysplasia (FMD) is a rare condition that can result in renal infarction. Treatment and long-term management of patients with this condition is controversial. We report the case of a patient with SRAD secondary to FMD who was treated by renal arterial stenting. A previous healthy 50-year-old white male presented to the emergency department with acute right flank pain. Blood pressure was 150/90 mmHg and serum creatinine was 1.6 mg/dL. A CT scan of the abdomen showed multifocal right renal infarction. The patient was started on anticoagulant regimen of heparin. Renal angiography showed the dissection of right renal artery and stenosis of mid-segment of right main renal artery and intrarenal branches. We decided to perform percutaneous balloon angioplasty and stenting for the purpose of dilating the stenotic renal artery, preventing recurrence of the disease and controlling hypertension and elevated creatinine. A dissected intimal flap was closed successfully by renal artery stenting and stenotic renal artery was dilated by stenting and balloon angioplasty. Five days after the procedure, he was discharged with warfarin. Three months later, he had normal renal function and blood pressure without antihypertensive medication was mildly elevated at 145/104 mmHg. Conclusively, stent implantation to renal artery dissection can be effective, reliable and feasible and can be an alternative to surgical treatment.


Subject(s)
Humans , Male , Middle Aged , Abdomen , Angiography , Angioplasty, Balloon , Blood Pressure , Constriction, Pathologic , Creatinine , Emergency Service, Hospital , Fibromuscular Dysplasia , Flank Pain , Heparin , Hypertension , Infarction , Recurrence , Renal Artery , Stents , Tomography, X-Ray Computed , Warfarin
5.
Korean Journal of Nephrology ; : 457-463, 2003.
Article in Korean | WPRIM | ID: wpr-37954

ABSTRACT

Renal infarction usually occurs in patients with atrial fibrillation, valvular heart disease, trauma, renal artery stenosis, atherosclerosis and coagulopathy. However it may occur rarely in patients without such underlying disease. We report on 3 patients who developed renal infarction and had no underlying disease. In two cases, renal artery thrombosis occured. And in the other case, renal artery dissection occured. All patients of the renal infarction experienced severe flank pain. And increased serum LDH, ALT and ALP was noted. The differential diagnosis of renal artery dissection and renal artery thrombosis was established by renal artery angiography. In two patients with renal artery thrombosis, anticoagulation therapy was performed. In the other patient with renal artery dissection, only conservative therapy was performed. All 3 patients of renal infarction preserved normal renal function. but developed hypertension. Two patients were given anti-hypertensive agents. In the other patient, hypertension was normalized spontaneously.


Subject(s)
Adult , Humans , Angiography , Antihypertensive Agents , Atherosclerosis , Atrial Fibrillation , Diagnosis, Differential , Flank Pain , Heart Valve Diseases , Hypertension , Infarction , Renal Artery , Renal Artery Obstruction , Thrombosis
6.
Korean Journal of Nephrology ; : 499-502, 2002.
Article in Korean | WPRIM | ID: wpr-149229

ABSTRACT

It is usually known that arterial dissection is associated with malignant hypertension, severe atherosclerosis or trauma. Marfan syndrome or Ehlers- Danlos syndrome may also be rare causes. However, as in this case, spontaneous arterial dissection without aortic dissection in normotensive men is rarely reported. A 39-year-old man presented with acute onset right flank pain with microscopic hematuria. Physical examination was unremarkable and his blood pressure was normal. Clinical impression was urolithiasis because he experienced two episodes of urolithiasis previously. IVP was not completed due to adverse reaction during study. Right renal infarction was diagnosed by contrast-enhanced computed tomography. To search for possible cardiac embolic disease, the patient underwent surface echocardiography, which was normal and a detailed evaluation for a thrombotic tendency was unremarkable. A renal arteriogram showed dissection of the main right renal artery with extension to renal artery branches and a wedge-shape perfusion defect in the distal part of the occluded artery. He received aorto-renal bypass surgery using his great saphenous vein. The patient developed hypertension 3 months later. To summary, we report a case of spontaneous renal artery dissection with renal infarction in a healthy man without hypertension.


Subject(s)
Adult , Humans , Arteries , Atherosclerosis , Blood Pressure , Echocardiography , Flank Pain , Hematuria , Hypertension , Hypertension, Malignant , Infarction , Marfan Syndrome , Multiple Endocrine Neoplasia Type 1 , Perfusion , Physical Examination , Renal Artery , Saphenous Vein , Urolithiasis
7.
Korean Journal of Nephrology ; : 831-836, 2002.
Article in Korean | WPRIM | ID: wpr-196167

ABSTRACT

Spontaneous renal artery dissection is an uncommon cause of renal infarction. Previous reports of spontaneous renal artery dissection has been associated with hypertension or fibromuscular dysplasia. We report herein the case of a previously healthy, normotensive patient with renal infarction due to spontaneous renal artery dissection who remained normotensive throughout his course without therapy. A previously healthy 31-year-old man with well- documented normotension had a sudden onset of right flank pain and delayed onset of elevation of lactic dehydrogenase, hematuria, and proteinuria. Thin section spiral computerized tomogram shows linear intraluminal filling defect suggesting intimal flap. Angiography shows dissection of main right renal artery. Six months later, he has remained well and normotensive without therapy. To our knowledge, this is the first case of spontaneous renal artery dissection in normotensive patients in Korea.


Subject(s)
Adult , Humans , Angiography , Fibromuscular Dysplasia , Flank Pain , Hematuria , Hypertension , Infarction , Korea , Oxidoreductases , Proteinuria , Renal Artery
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